NP-MRD: Showing NP-Card for 3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene (NP0043063)

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Record Information

Version

2.0

Created at

2021-06-21 00:34:11 UTC

Updated at

2021-06-30 00:18:32 UTC

NP-MRD ID

NP0043063

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene

Provided By

JEOL Database JEOL Logo

Description

CHEMBL3103099 belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene is found in Flueggea virosa. 3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene was first documented in 2014 (Chao, C.-H., et al.). Based on a literature review very few articles have been published on CHEMBL3103099.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102343D          

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M  END

     RDKit          3D

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  Mrv1652306212102343D          

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 10 30  1  0  0  0  0
  7 26  1  0  0  0  0
  4 25  1  0  0  0  0
 17 40  1  0  0  0  0
 14 33  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 21 45  1  0  0  0  0
 21 46  1  0  0  0  0
 21 47  1  0  0  0  0
 15 36  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
  9 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0043063

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])C([H])([H])C([H])([H])[C@]2(C3=C([H])C(OC([H])([H])[H])=C(C([H])=C3C([H])=C([H])[C@]2([H])C1(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O2/c1-12-10-13-6-7-16-18(2,3)17(20)8-9-19(16,4)14(13)11-15(12)21-5/h6-7,10-11,16-17,20H,8-9H2,1-5H3/t16-,17-,19+/m1/s1

> <INCHI_KEY>
VOAVINJXKSDKJS-LMMKCTJWSA-N

> <FORMULA>
C19H26O2

> <MOLECULAR_WEIGHT>
286.415

> <EXACT_MASS>
286.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.15063551162085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4aR,10aS)-6-methoxy-1,1,4a,7-tetramethyl-1,2,3,4,4a,10a-hexahydrophenanthren-2-ol

> <ALOGPS_LOGP>
4.63

> <JCHEM_LOGP>
4.157780378333333

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.699250750205426

> <JCHEM_PKA_STRONGEST_BASIC>
-2.930347721860146

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
87.6725

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.73e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aR,10aS)-6-methoxy-1,1,4a,7-tetramethyl-2,3,4,10a-tetrahydrophenanthren-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -4.5264   -0.9375   -3.4360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5052   -0.2782   -4.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2699   -0.1689   -3.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9332   -0.6813   -2.3271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6391   -0.5213   -1.7956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3301    0.1546   -2.5687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0035    0.6547   -3.8317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2995    0.5053   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6315    1.0588   -5.7039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6998    0.3181   -2.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554    0.1739   -0.7597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365   -0.1351    0.2175 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2902   -0.4586    1.6864 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0590    0.7608    2.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2495   -1.6632    1.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0200   -0.6628    2.5610 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3817   -1.1017    3.8698 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9792   -1.6538    1.9713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4017   -1.2758    0.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2134   -1.1219   -0.4297 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3492   -2.5264   -0.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383   -0.4145   -2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4388   -0.9182   -4.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2690   -1.9866   -3.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6728   -1.2253   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7497    1.1723   -4.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9241    0.2500   -6.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475    1.7849   -5.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7732    1.5720   -6.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4868    0.5722   -2.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.3248   -0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050    0.8291    0.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.9284    1.7613 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4680    1.6799    2.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.6168    3.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0555   -1.6116    1.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -1.6972    2.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7434   -2.6210    1.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4877    0.3037    2.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313   -1.1514    4.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700   -1.6894    2.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -2.6716    2.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1045   -2.0398    0.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656   -0.3341    0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3638   -3.0970   -1.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2835   -2.4800   -1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348   -3.1350    0.1206 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 12  1  0
 18 16  1  0
 18 19  1  0
  5  4  2  0
  6  7  2  0
  7  8  1  0
  8  3  2  0
  3  4  1  0
 16 13  1  0
 16 17  1  0
 20  5  1  0
 13 14  1  1
 12 11  1  0
 20 21  1  6
 11 10  2  0
 13 15  1  0
 10  6  1  0
 12 32  1  1
  5  6  1  0
  8  9  1  0
 13 12  1  0
  3  2  1  0
 20 19  1  0
  2  1  1  0
 18 41  1  0
 18 42  1  0
 16 39  1  1
 19 43  1  0
 19 44  1  0
 11 31  1  0
 10 30  1  0
  7 26  1  0
  4 25  1  0
 17 40  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.526  -0.938  -3.436  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.505  -0.278  -4.172  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.270  -0.169  -3.587  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.933  -0.681  -2.327  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.639  -0.521  -1.796  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.330   0.155  -2.569  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.004   0.655  -3.832  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.300   0.505  -4.346  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.632   1.059  -5.704  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.700   0.318  -2.068  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.955   0.174  -0.760  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.837  -0.135   0.218  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.290  -0.459   1.686  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.059   0.761   2.272  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.249  -1.663   1.796  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.020  -0.663   2.561  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.382  -1.102   3.870  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.979  -1.654   1.971  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.402  -1.276   0.554  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.213  -1.122  -0.430  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.349  -2.526  -0.764  0.00  0.00           C+0
HETATM   22  H   UNK     0      -4.738  -0.415  -2.498  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.439  -0.918  -4.040  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.269  -1.987  -3.257  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.673  -1.225  -1.753  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.750   1.172  -4.422  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.924   0.250  -6.381  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.447   1.785  -5.629  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.773   1.572  -6.150  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.487   0.572  -2.770  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.968   0.325  -0.402  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.305   0.829   0.316  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.013   0.928   1.761  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.468   1.680   2.188  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.289   0.617   3.334  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.055  -1.612   1.057  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.728  -1.697   2.783  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.743  -2.621   1.677  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.488   0.304   2.681  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.431  -1.151   4.401  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.870  -1.689   2.612  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.575  -2.672   2.003  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.104  -2.040   0.199  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.966  -0.334   0.602  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.364  -3.097  -1.373  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.284  -2.480  -1.333  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.535  -3.135   0.121  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    3    1                                                       
CONECT    3    8    4    2                                                  
CONECT    4    5    3   25                                                  
CONECT    5    4   20    6                                                  
CONECT    6    7   10    5                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   27   28   29                                             
CONECT   10   11    6   30                                                  
CONECT   11   12   10   31                                                  
CONECT   12   20   11   32   13                                             
CONECT   13   16   14   15   12                                             
CONECT   14   13   33   34   35                                             
CONECT   15   13   36   37   38                                             
CONECT   16   18   13   17   39                                             
CONECT   17   16   40                                                       
CONECT   18   16   19   41   42                                             
CONECT   19   18   20   43   44                                             
CONECT   20   12    5   21   19                                             
CONECT   21   20   45   46   47                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    4                                                            
CONECT   26    7                                                            
CONECT   27    9                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   14                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   15                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   17                                                            
CONECT   41   18                                                            
CONECT   42   18                                                            
CONECT   43   19                                                            
CONECT   44   19                                                            
CONECT   45   21                                                            
CONECT   46   21                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   98    0
END

RDKit          3D

47 49  0  0  0  0  0  0  0  0999 V2000
   -4.5264   -0.9375   -3.4360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5052   -0.2782   -4.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2699   -0.1689   -3.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9332   -0.6813   -2.3271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6391   -0.5213   -1.7956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3301    0.1546   -2.5687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0035    0.6547   -3.8317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2995    0.5053   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6315    1.0588   -5.7039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6998    0.3181   -2.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554    0.1739   -0.7597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365   -0.1351    0.2175 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2902   -0.4586    1.6864 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0590    0.7608    2.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2495   -1.6632    1.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0200   -0.6628    2.5610 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3817   -1.1017    3.8698 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9792   -1.6538    1.9713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4017   -1.2758    0.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2134   -1.1219   -0.4297 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3492   -2.5264   -0.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383   -0.4145   -2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4388   -0.9182   -4.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2690   -1.9866   -3.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6728   -1.2253   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7497    1.1723   -4.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9241    0.2500   -6.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475    1.7849   -5.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7732    1.5720   -6.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4868    0.5722   -2.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.3248   -0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050    0.8291    0.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.9284    1.7613 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4680    1.6799    2.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.6168    3.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0555   -1.6116    1.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -1.6972    2.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7434   -2.6210    1.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4877    0.3037    2.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313   -1.1514    4.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700   -1.6894    2.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -2.6716    2.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1045   -2.0398    0.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656   -0.3341    0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3638   -3.0970   -1.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2835   -2.4800   -1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348   -3.1350    0.1206 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 12  1  0
 18 16  1  0
 18 19  1  0
  5  4  2  0
  6  7  2  0
  7  8  1  0
  8  3  2  0
  3  4  1  0
 16 13  1  0
 16 17  1  0
 20  5  1  0
 13 14  1  1
 12 11  1  0
 20 21  1  6
 11 10  2  0
 13 15  1  0
 10  6  1  0
 12 32  1  1
  5  6  1  0
  8  9  1  0
 13 12  1  0
  3  2  1  0
 20 19  1  0
  2  1  1  0
 18 41  1  0
 18 42  1  0
 16 39  1  1
 19 43  1  0
 19 44  1  0
 11 31  1  0
 10 30  1  0
  7 26  1  0
  4 25  1  0
 17 40  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₂

Average Mass

286.4150 Da

Monoisotopic Mass

286.19328 Da

IUPAC Name

(2R,4aR,10aS)-6-methoxy-1,1,4a,7-tetramethyl-1,2,3,4,4a,10a-hexahydrophenanthren-2-ol

Traditional Name

(2R,4aR,10aS)-6-methoxy-1,1,4a,7-tetramethyl-2,3,4,10a-tetrahydrophenanthren-2-ol

CAS Registry Number

Not Available

SMILES

[H]O[C@]1([H])C([H])([H])C([H])([H])[C@]2(C3=C([H])C(OC([H])([H])[H])=C(C([H])=C3C([H])=C([H])[C@]2([H])C1(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C19H26O2/c1-12-10-13-6-7-16-18(2,3)17(20)8-9-19(16,4)14(13)11-15(12)21-5/h6-7,10-11,16-17,20H,8-9H2,1-5H3/t16-,17-,19+/m1/s1

InChI Key

VOAVINJXKSDKJS-LMMKCTJWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Flueggea virosa	JEOL database	Chao, C.-H., et al, J. Nat. Prod. 77, 22 (2014)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Phenanthrene
Hydrophenanthrene
Naphthalene
Anisole
Alkyl aryl ether
Benzenoid
Cyclic alcohol
Secondary alcohol
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.63	ALOGPS
logP	4.16	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	14.7	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	87.67 m³·mol⁻¹	ChemAxon
Polarizability	34.15 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

31125045

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76317304

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chao, C.-H., et al. (2014). Chao, C.-H., et al, J. Nat. Prod. 77, 22 (2014). J. Nat. Prod..

Showing NP-Card for 3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene (NP0043063)

MOL for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

3D MOL for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

3D SDF for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

3D-SDF for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

PDB for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

3D PDB for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

SMILES for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

INCHI for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

Structure for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)

3D Structure for NP0043063 (3alpha-hydroxy-12-methoxy-13-methyl-ent-podocarp-6,8,11,13-tetraene)